Medical Device Regulations in Latin America, Canada and USA
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International Medical Device Conferences

A list of international medical device conferences, medical device meetings and medical device training courses for the medical device industry and in vitro diagnostic medical device industry.

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DATETITLELOCATIONORGANISER
March 2010
1-3 Medical Devices Summit 2010 Boston, MA, USA Opal Events
+1 212 532 9898
1-3 Principles of European Medical Technology Regulatory Affairs The Clayton Hotel, Galway, Ireland TOPRA
+44(0) 20 7510 2560
2Advanced Process Auditing Techniques for Medical Device/Pharma Quality SystemsOn-line EventCompliance Online
+1 650 620 3915
3EU's MDD Mod 5 Changes due March 2010 - Impact on CE-mark ComplianceOn-line EventCompliance Online
+1 650 620 3915
3-5Advances and Debates in Clinical Obstetrics and GynaecologyHurghada, EgyptEgyptian Society of Gynaecology and Obstetrics
+2 011 700 9620
18How to implement parametric release in EO sterilisation - Practical approachOn-line EventCompliance Online
+1 650 620 3915
18-19 Innovative Market Access Strategies for Medical Devices & Technologies Budapest, Hungary NextLevel Pharma
+421 232 662 621
19Validating Radiation Sterilisation for medical device industriesOn-line EventCompliance Online
+1 650 620 3915
23-24Sterilisation for Medical DevicesLondon, UKInforma Lifesciences
+44 (0)20 7017 7481
24Overview of the Medical Device Risk Management Standard - ISO 14971On-line EventCompliance Online
+1 650 620 3915
24Clinical Evaluation Reports (CERs) Required for All Classes of Medical Devices in EuropeOn-line EventCompliance Online
+1 650 620 3915
26Regulatory Requirements for Medical Device Calibration ProgramsOn-line EventCompliance Online
+1 650 620 3915
31ISO 13485: 2003 for Medical Devices - How it differs to ISO 9001: 2008 and FDA part 820 requirementsOn-line EventCompliance Online
+1 650 620 3915



DATETITLELOCATIONORGANISER
April 2010
9ISO 14971: 2007 and the CE MarkOn-line EventCompliance Online
+1 650 620 3915
12-14 7th Annual World Health Care Congress (WHCC) National Harbor, MD, USA World Congress
+1 781 939 2587
13-14Clinical Evaluations and InvestigationsLondon, UKInforma Life Sciences
+44 (0)20 7017 7481
14Reducing Ethylene Oxide (EO) Sterilisation costs while maintaining regulatory complianceOn-line EventCompliance Online
+1 650 620 3915
21-22MEDTEC France 2010Besançon, FranceCanon Communications
+33 (0)1 7748 1007
22What are DHF, DMR and DHR? - The FDA Quality Systems Regulations Records ExplainedOn-line EventCompliance Online
+1 650 620 3915
29The FDA's New Emphasis on Supplier Controls - Is Your Company Ready?On-line EventCompliance Online
+1 650 620 3915



DATETITLELOCATIONORGANISER
May 2010
11-13 Management of Regulatory Affairs and its Contribution to the Medical Technology Lifecycle Cranfield University, UK Cranfield University
+44 (0)1234 754192
20-21Device Research - Regulations and Guidelines for Device Clinical ResearchSan Francisco, CA, USASociety of Clinical Research Associates
+1 800SoCRA92

DATETITLELOCATIONORGANISER
June 2010
22-24Medical Device & IVD Regulations in Asia-PacificLondon, UKInforma Life Sciences
+44 (0)20 7017 7481

DATETITLELOCATIONORGANISER
September 2010
16-18The Pan African Health Expo and Conference 2010South AfricaFair Consultants SA
+27 21 713 3360

DATETITLELOCATIONORGANISER
October 2010
82010 RAPS Annual Conference & ExhibitionSan Jose, CA, USARegulatory Affairs Professionals Society (RAPS)
+1 301 770 2920
18-20AdvaMed 2010: The MedTech ConferenceWashington, DC, USAAdvaMed
+1 202 434 7213